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rs779874042

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs779874042(C;T)
Make rs779874042(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position178563493
GeneTTN, TTN-AS1
is asnp
is mentioned by
dbSNPrs779874042
ebirs779874042
HLIrs779874042
Exacrs779874042
Varsomers779874042
Maprs779874042
PheGenIrs779874042
hapmaprs779874042
1000 genomesrs779874042
hgdprs779874042
ensemblrs779874042
gopubmedrs779874042
geneviewrs779874042
scholarrs779874042
googlers779874042
pharmgkbrs779874042
gwascentralrs779874042
openSNPrs779874042
23andMers779874042
23andMe allrs779874042
SNP Nexus

SNPshotrs779874042
SNPdbers779874042
MSV3drs779874042
GWAS Ctlgrs779874042
Max Magnitude0
ClinVar
Risk rs779874042(A,T;A,T)
Alt rs779874042(A,T;A,T)
Reference rs779874042(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TTN TTN-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.179428220C>A
CLNSRC
CLNACC RCV000184272.2,